JP2022543231A5 - - Google Patents

Info

Publication number
JP2022543231A5
JP2022543231A5 JP2022506574A JP2022506574A JP2022543231A5 JP 2022543231 A5 JP2022543231 A5 JP 2022543231A5 JP 2022506574 A JP2022506574 A JP 2022506574A JP 2022506574 A JP2022506574 A JP 2022506574A JP 2022543231 A5 JP2022543231 A5 JP 2022543231A5
Authority
JP
Japan
Prior art keywords
optionally substituted
bispecific compound
hydrogen
group
pharmaceutically acceptable
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2022506574A
Other languages
English (en)
Japanese (ja)
Other versions
JP2022543231A (ja
JP7636388B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2020/044815 external-priority patent/WO2021026109A1/en
Publication of JP2022543231A publication Critical patent/JP2022543231A/ja
Publication of JP2022543231A5 publication Critical patent/JP2022543231A5/ja
Application granted granted Critical
Publication of JP7636388B2 publication Critical patent/JP7636388B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2022506574A 2019-08-05 2020-08-04 サイクリン依存性キナーゼ7(cdk7)の分解誘導剤およびその使用 Active JP7636388B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962882958P 2019-08-05 2019-08-05
US62/882,958 2019-08-05
PCT/US2020/044815 WO2021026109A1 (en) 2019-08-05 2020-08-04 Degraders of cyclin-dependent kinase 7 (cdk7) and uses thereof

Publications (3)

Publication Number Publication Date
JP2022543231A JP2022543231A (ja) 2022-10-11
JP2022543231A5 true JP2022543231A5 (enExample) 2023-08-02
JP7636388B2 JP7636388B2 (ja) 2025-02-26

Family

ID=74503218

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022506574A Active JP7636388B2 (ja) 2019-08-05 2020-08-04 サイクリン依存性キナーゼ7(cdk7)の分解誘導剤およびその使用

Country Status (8)

Country Link
US (1) US12491251B2 (enExample)
EP (1) EP4010336B1 (enExample)
JP (1) JP7636388B2 (enExample)
CN (1) CN114174281B (enExample)
AU (1) AU2020324408B2 (enExample)
CA (1) CA3149374A1 (enExample)
ES (1) ES3031581T3 (enExample)
WO (1) WO2021026109A1 (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10870651B2 (en) 2014-12-23 2020-12-22 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
CN107427521B (zh) 2015-03-27 2021-08-03 达纳-法伯癌症研究所股份有限公司 细胞周期蛋白依赖性激酶的抑制剂
EP3810132A4 (en) 2018-06-25 2022-06-22 Dana-Farber Cancer Institute, Inc. TAIRE FAMILY KINASE INHIBITORS AND RELATED USES
CN113164477A (zh) 2018-12-14 2021-07-23 达纳-法伯癌症研究所股份有限公司 C-jun-n-末端激酶的吡唑并吡啶抑制剂及其用途
EP3902542A4 (en) 2018-12-28 2022-09-07 Dana-Farber Cancer Institute, Inc. CYCLIN DEPENDENT KINASE 7 INHIBITORS AND USES THEREOF
CA3166135A1 (en) * 2019-12-24 2021-07-01 Dana-Farber Cancer Institute, Inc. The combination of cyclin dependent kinase 7 inhibitor and immunotherapy for treatment of cancer
CN117242060B (zh) 2021-01-13 2026-07-17 蒙特罗莎治疗股份有限公司 异吲哚啉酮化合物
CA3217792A1 (en) 2021-05-07 2022-11-10 Kymera Therapeutics, Inc Cdk2 degraders and uses thereof
CN113234081A (zh) * 2021-05-27 2021-08-10 东南大学 一种吡咯并吡唑衍生物与dmpeda做脲的制备方法
WO2022248682A1 (en) * 2021-05-28 2022-12-01 Qurient Co., Ltd. Compounds for degradation of cyclin-dependent kinase 7 (cdk7)
CN116396295A (zh) * 2023-04-04 2023-07-07 合肥工业大学 一种基于protac的plk1降解剂的合成方法
WO2025252190A1 (en) * 2024-06-07 2025-12-11 Cullgen Inc. Targeted degraders of werner syndrome recq helicase
CN119119072B (zh) * 2024-08-23 2025-10-03 武汉大学 一种用于检测和降解ERα的诊疗一体化ERαPROTACs化合物及其制备方法与应用

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2416527C (en) 2000-08-10 2009-12-22 Pharmacia Italia S.P.A. Bicyclo-pyrazoles active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them
US7968569B2 (en) 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
US9345705B2 (en) 2011-09-15 2016-05-24 Merck Sharp & Dohme Corp. Compositions and methods for treating cancer
WO2013070688A1 (en) 2011-11-11 2013-05-16 Yale University Reprogramming urokinase into an antibody-recruiting anticancer agent
KR102438072B1 (ko) 2012-01-12 2022-08-31 예일 유니버시티 E3 유비퀴틴 리가아제에 의한 표적 단백질 및 다른 폴리펩티드의 증진된 분해를 위한 화합물 및 방법
US10870651B2 (en) * 2014-12-23 2020-12-22 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
AU2016232705C1 (en) * 2015-03-18 2021-06-17 Arvinas, Inc. Compounds and methods for the enhanced degradation of targeted proteins
AU2016281225B2 (en) * 2015-06-15 2020-10-15 Ube Corporation Substituted dihydropyrrolopyrazole derivative
BR112018008918A8 (pt) 2015-11-02 2019-02-26 Univ Yale compostos de quimera proteólise dirigida e métodos para preparação e uso dos mesmos
AU2017254702B2 (en) 2016-04-22 2020-12-24 Dana-Farber Cancer Institute, Inc. Degradation of cyclin-dependent kinase 9 (CDK9) by conjugation of CDK9 inhibitors with E3 ligase ligand and methods of use
CN121974842A (zh) * 2016-05-10 2026-05-05 C4医药公司 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体
CA3045037A1 (en) * 2016-12-08 2018-06-14 Icahn School Of Medicine At Mount Sinai Compositions and methods for treating cdk4/6-mediated cancer
CN109516989B (zh) 2017-09-17 2021-12-31 上海美志医药科技有限公司 一类抑制并降解cdk的化合物

Similar Documents

Publication Publication Date Title
JP2023520333A5 (enExample)
JP2022512900A5 (enExample)
JP5324574B2 (ja) C型肝炎の治療に有用な化合物の合成方法
IL281503A (en) Preparations and methods for preventing Arginase activity
US20090041716A1 (en) Crystalline form of methyl ((1s)-1-(((2s)-2-(5-(4'-(2-((2s)-1((2s)-2-((methoxycarbonyl)amino)-3-methylbutanoyl)-2-pyrrolidinyl)-1h-imidazol-5-yl)-4-biphenylyl)-1h-imidazol-2-yl)-1-pyrrolidinyl)carbonyl)-2-methylpropyl)carbamate dihydrochloride salt
IL296994A (en) Compounds and uses thereof
JP2024519140A5 (enExample)
JP2009530424A5 (enExample)
RU2020108523A (ru) Гетероарил-замещенные бета-гидроксиэтиламины для применения для лечения гипергликемии
JP2005505507A (ja) 抗感染活性を有するイソキノリン化合物
CZ20031380A3 (cs) LFA-1 Antagonistické sloučeniny
JP2010510301A (ja) 化合物
JP2022510505A5 (enExample)
JP2024521919A5 (enExample)
JP2000503999A (ja) ジスタマイシン誘導体、その調製方法、および抗腫瘍および抗ウイルス剤としてのその使用
JP2000510129A (ja) ジスタマイシン誘導体、その調製方法並びに抗腫瘍薬及び抗ウイルス薬としてのその使用
NL1027545C2 (nl) Chinolonen als antibacteriele middelen.
US20250243211A1 (en) Processes and intermediates for producing diazaspiro lactam compounds
EP3578179A1 (en) Process for the preparation of cyclic depsipeptides
AU2020348825B2 (en) Heterocyclic amide compound, pharmaceutically acceptable salt thereof, and preparation method therefor and use thereof
CN105399737B (zh) 噁唑烷酮类化合物及其用途
JP4149172B2 (ja) インテグリンと受容体との結合を阻害するカルボン酸誘導体
JP2003515586A (ja) アクリロイルペプチド誘導体、その調製法、およびその抗腫瘍薬としての使用
HUT75114A (en) 1-oxo-2-(phenylsulfonyl-amino)-pentylpiperidine derivatives, process for producing them and pharmaceutical use of them
JPH01199983A (ja) 新規珪素含有ペプチド類、それらの製法および用途